Biotechnology - Gene Cloning

Gene Cloning

Biotechnology

Gene Cloning

Making multiple copies of a single gene

Step 1: Forming recombinant DNA

Step 2: Transformation (In vivo amplification)

Step 3: Selection

http://tainano.com/Molecular%20Biology%20Glossary.files/image053.gif

Animation

Introduces gene cloning including information on forming a recombinant and transformation

http://highered.mcgraw-hill.com/olc/dl/120078/micro10.swf

http://tainano.com/Molecular%20Biology%20Glossary.files/image053.gif

Cloning Vector

Plasmid: small circular DNA found in bacterial cells that is not the chromosomal DNA

Cloning vector: a plasmid into which the

gene of interest is introduced

Contains a number of specific genes useful in selection

Cloning vector componentsOriampR genelacZ generestriction sites

Activity: Gene CloningIn this activity you will determine the

function of the ampR and lacZ gene and explain its use in gene cloning

Cloning vector components

Replication origin (ori): allows plasmid to replicate in the host cell

Cloning vector components

Antibiotic resistance (ampR) gene: allows cells to be resistance to ampicillin (an antibiotic)

Selection for host cells that have resistance

Thus, selecting for transformation

Cloning vector components

β-galactosidase (LacZ) gene: enzyme produced will change a clear substrate called X-gal into a blue product

β-galactosidase Reactionβ-gal acts on X-Gal (a clear soluble

substrate) to produce a blue precipitate

X-gal (colourless)

5-bromo-4-chloro-3-hydroxyindole galactose

5,5'-dibromo-4,4'-dichloro-indigo, an intensely blue product which is insoluble

Spontaneous dimerization & oxidation

hydrolysis

LacZ question

The cloning vector on the right has a functioning lacZ gene.

What will be the colour of the bacterial cell if it has this plasmid and is grown in X-gal?

What would be the colour of the bacterial cell if it does not have this plasmid and is grown in X-gal?

Cloning vector components

Cloning site:Where gene of

interest will be inserted (ligated)

Where transcription can occur because contains an upstream promoter

Step 1: Forming Recombinant DNA

Where would you insert the DNA of interest so that you can “see” it in the bacterial cell (assume cells are grown in X-gal)?

Step 1: Forming Recombinant DNA

Ligate the gene of interest into the vector such that it interrupts the lacZ gene

Thus β–galactosidase is not made

Question: What colour would the bacterial cells be if grown in X-gal?

Step 2: Transformation

Transform recombinant DNA into bacterial cell

As bacterial cells multiply, the gene of interest will be replicated with each cell

Step 2: Transformation

Bacteria grown in flasks of liquid medium

Incubate at optimal growing temperature

http://photos.news.wisc.edu/photos/8402/original/Shen_bacteria_flask08_8579.jpg?1286762168

Step 3: Selection

Selection: Identify colonies of bacteria containing the recombinant DNA with gene of interest

Possible bacterial clone products:A. bacteria without vectorB. bacteria with vector without the geneC. bacteria with vector with the gene of

interest

Step 3: Selection

Plating: taking a sample of the bacteria and growing them on plates

Plates have a medium containing:AntibioticsX-gal

Selection Mechanism: Antibiotic Resistance

Select for bacterial clones that contain a vector (select for proper transformation)

Bacteria are grown on Petri plate containing a specific antibiotic (e.g. ampicillin)

Antibiotic Resistance

Vector confers antibiotic resistant to bacteria because the vector contains an antibiotic resistant gene (ampR)

Only bacterial cells that properly transformed the vector will live and grow on the plate

Selection for successful transformation

http://www.biotechlearn.org.nz/var/biotechlearn/storage/images/themes/from_genes_to_genomes/images/bacterial_transformation/4063-1-eng-AU/bacterial_transformation_large.jpg

Selection Mechanisms: β-galactosidase Screening

Select for bacterial clones that contain a vector with gene of interest (select for proper ligation)

Bacteria are grown on Petri plates containing X-Gal

Selection for successful ligation

Vectors contain lac Z gene that codes for the β-galactosidase (β-gal)

Vectors that have the DNA insert won’t have a functional β-gal enzyme

These bacteria, when grown in X-gal, cannot process it and stays white

Selection for successful ligation

Bacteria which accepted a vector WITHOUT the DNA of interest will have a working lacZ gene

Gene codes for working β-gal enzyme which will process X-gal into a blue product

Possible Transformation ResultsLB Medium additions

No vector Cloning vector

Recombinant DNA

Amp No growth White White

X-gal White Blue White

Amp + X-gal

No growth Blue White

Fig. 20.1

Animation: Gene cloning

http://www.sumanasinc.com/webcontent/animations/content/plasmidcloning.html (includes antibiotic resistance info)

Cloning Application: Flavr Savr Tomatoes

First genetically modified produce Genetically modified tomatoes that

suppressed a gene responsible for fruit ripening

Process required cloning the gene and transforming a reverse-orientation copy which would have inhibitory effects.

Video CBC: The science and controversy behind the world’s first genetically modified produce (watch first 2 minutes of 18:27): http://www.cbc.ca/archives/categories/economy-business/agriculture/genetically-modified-food-a-growing-debate/introducing-the-flavr-savr-tomato.html

http://ucanr.org/repository/CAO/landingpage.cfm?article=ca.v054n04p6&fulltext=yes

Cloning Application: Bt Plants

Bacillus Thuringiensis a bacterium used as a biological pesticide

Bt gene is cloned into plants so that they will be resistant to pests